Established in 1836, Acino, part of Arcera, is a pharmaceutical company headquartered in Zurich, with a clear focus on selected markets in the Middle East, Africa, and Latin America, as well as Ukraine and Eurasian countries. With over 3,000 people across 90 countries, we deliver quality pharmaceuticals to promote affordable healthcare in these emerging markets. We also leverage our high-quality pharmaceutical manufacturing capabilities and network to supply leading companies through contract manufacturing and out-licensing.
Acino is part of Arcera, a diversified life sciences holding company, established by ADQ in Abu Dhabi in 2024 with the purpose to advance innovation in line with the Emirate’s 2030 vision for the sector and beyond.
We are constantly expanding our market position with a future-oriented international business strategy. Therefore, we are looking for a dedicated and motivated person to strengthen our team in Munich, Germany.
Qualified Person 100% (w/m/d)
Major Accountabilities:
- Certify that each batch of medical product is manufactured and tested in accordance with Marketing Authorization requirements, GMP and applicable regulations.
- Oversee batch release activities, ensuring all deviations and CAPAs are properly investigated and documented
- Maintain oversight of the supply chain to prevent distribution of non-compliant or falsified medicines.
- Ensure compliance of third-party manufacturers and suppliers with GMP standards.
- Ensure batch certification is performed in accordance with GMP requirements and ethical standards. Maintain up-to-date knowledge of legal requirements and technical standards
- Certify and release batches of medicinal products
- Contribute in a team of quality professionals
Your Profile:
- University degree in Pharmacy, Chemistry or related life sciences
- Recognized QP status and valid authorization from relevant health authorities.
- Proven experience in pharmaceutical industry and in pharmacovigilance (GVP)
- Fluent in German and English, with excellent written and verbal communication skills
- Strong understanding of regulatory requirements and quality standards
- Strong computer literacy and familiarity with digital QMS and LIMS platforms.
- Ability to drive change and foster a culture of quality and compliance.
We offer a very attractive working environment within a highly motivated team with excellent working conditions. You can expect the following benefits:
- A position with a stable and resilient pharmaceutical company
- An international working environment within a continuously growing organization
- Interesting and highly diverse responsibilities that provide a strong foundation for further career development in the pharmaceutical industry
- An attractive salary package
- A generous pension scheme
- Free parking facilities
- Complimentary coffee, tea, and fresh fruit
- Attractive additional benefits, such as subsidized lunches and corporate benefit programs
This is the opportunity to join a very dynamic organization, where decisions are taken fast and where you can actively participate in shaping our future. If you are interested in this role we are looking forward to hearing from you.
Please apply via our Homepage.
Job Types: Full-time, Permanent
Work Location: Hybrid remote in 80804 München
